@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP73946.RAWnHqXXTdbF_It_g6UvJVVSts31UGJLjnSBXGd2lC9mo> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP73946.RAWnHqXXTdbF_It_g6UvJVVSts31UGJLjnSBXGd2lC9mo130_head {
  this: np:hasAssertion dgn-np:NP73946.RAWnHqXXTdbF_It_g6UvJVVSts31UGJLjnSBXGd2lC9mo130_assertion;
    np:hasProvenance dgn-np:NP73946.RAWnHqXXTdbF_It_g6UvJVVSts31UGJLjnSBXGd2lC9mo130_provenance;
    np:hasPublicationInfo dgn-np:NP73946.RAWnHqXXTdbF_It_g6UvJVVSts31UGJLjnSBXGd2lC9mo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP73946.RAWnHqXXTdbF_It_g6UvJVVSts31UGJLjnSBXGd2lC9mo130_assertion a np:Assertion .
  
  dgn-np:NP73946.RAWnHqXXTdbF_It_g6UvJVVSts31UGJLjnSBXGd2lC9mo130_provenance a np:Provenance .
  
  dgn-np:NP73946.RAWnHqXXTdbF_It_g6UvJVVSts31UGJLjnSBXGd2lC9mo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP73946.RAWnHqXXTdbF_It_g6UvJVVSts31UGJLjnSBXGd2lC9mo130_assertion {
  miriam-gene:2952 a ncit:C16612 .
  
  lld:C1168401 a ncit:C7057 .
  
  dgn-gda:DGN34de116112b21821069bf73a92c6158e sio:SIO_000628 miriam-gene:2952, lld:C1168401;
    a sio:SIO_001122 .
}

dgn-np:NP73946.RAWnHqXXTdbF_It_g6UvJVVSts31UGJLjnSBXGd2lC9mo130_provenance {
  dgn-np:NP73946.RAWnHqXXTdbF_It_g6UvJVVSts31UGJLjnSBXGd2lC9mo130_assertion dcterms:description
      "[the findings suggested that the genetic polymorphisms studied are predictors of risk and are also associated with tumor recurrence, since they are important for determining the parameters associated with tumor progression and poor outcomes in HNSCC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
    sio:SIO_000772 miriam-pubmed:19442564;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^xsd:date .
  
  dgn-void:source_evidence_literature a eco:ECO_0000212;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}

dgn-np:NP73946.RAWnHqXXTdbF_It_g6UvJVVSts31UGJLjnSBXGd2lC9mo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:36+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}